Issued to Acacia Pharma Ltd. Application reviewed but not approved; deficiencies must be corrected.
Issued
October 5, 2018Application
NDA 505b1 • 209510
Product
BARHEMSYS
Company
Acacia Pharma Ltd
Review center
Other
Stage
Final Decision
Response due
December 31, 2020
Assyro regulatory brief
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FDA's complete response letter contains source-text evidence related to Labeling, packaging, and proprietary name, Facility inspection and CGMP compliance. Theme counts identify where the letter discusses a topic; they do not replace review of the exact redacted letter.
Review the exact redacted FDA letter and address each stated deficiency before resubmission.
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Application reviewed but not approved; deficiencies must be corrected. Requires resubmission addressing deficiencies. FDA issued this letter to Acacia Pharma Ltd on October 5, 2018.
NDA 209510 is the application under which FDA issued this complete response letter for BARHEMSYS to Acacia Pharma Ltd. It was reviewed by FDA Other. The letter is dated October 5, 2018.
FDA will not approve the application in its present form. The sponsor can resubmit after addressing every deficiency listed in the letter — which starts a Class 1 (two-month) or Class 2 (six-month) resubmission review clock — withdraw the application, or request an opportunity for a hearing.